A citation-based method for searching scientific literature

Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Times Cited: 504

Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
Times Cited: 134

List of shared articles

Times cited

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021

Variants of uncertain significance in prenatal microarrays: a retrospective cohort study.
A H Mardy, A P Wiita, B V Wayman, K Drexler, T N Sparks, M E Norton. BJOG 2021

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
Annie Sy Hui, Matthew Hoi Kin Chau, Yiu Man Chan, Ye Cao, Angel Hw Kwan, Xiaofan Zhu, Yvonne K Kwok, Zihan Chen, Terence T Lao, Kwong Wai Choy,[...]. Acta Obstet Gynecol Scand 2021

Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.
Valeria Orlando, Viola Alesi, Gianluca Di Giacomo, Michela Canestrelli, Chiara Calacci, Anna Maria Nardone, Giusy Calvieri, Maria Teresa Liambo, Ester Sallicandro, Silvia Di Tommaso,[...]. Reprod Sci 2021

What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?
Idit Maya, Amihood Singer, Hagith Yonath, Adi Reches, Shlomit Rienstein, Sharon Zeligson, Shay Ben Shachar, Lena Sagi-Dain. Acta Obstet Gynecol Scand 2020

The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations.
Yael Pasternak, Yair Daykan, Tamar Tenne, Eyal Reinstein, Netanella Miller, Gil Shechter-Maor, Idit Maya, Tal Biron-Shental, Rivka Sukenik Halevy. J Matern Fetal Neonatal Med 2020